Category Archives: Drugs

Back to the Clinic

I had my regular ALS clinic appointment last week. I go every three months, which is recommended based on my level of progression. It’s not an uplifting place, but I’m learning to prepare myself and to control my reactions, regardless of what the clinicians might tell me. Having Rob there is crucial. The one time he couldn’t make it is the one time I ended up sobbing, and it took me a week to get back to normal.

Here’s how the appointment goes. I start out by getting weighed. That means wheeling my chair onto the scale to get the weight of both of us. Then I hop out (just kidding! I get out slowly, with help) and they weigh the chair alone. This brings to mind a new mom weighing a baby by holding it in her arms, and then weighing herself without it, and that thought leads to another thought and then another and I find myself wondering what I would be doing right then if I didn’t have ALS.

Then the nurse comes in and asks a series of questions called The Functional Rating Scale to determine how far I’ve progressed since I was last there. Yes, that’s right. They’re asking me. Read More>

An Underfunded Disease

“ALS is not an incurable disease.  It is an underfunded disease.”  – Stan Appel, M.D.

Last year, my husband Rob gathered a huge team of people to participate in the Napa Valley Ride to Defeat ALS. The event was held in September in Yountville, California on a gorgeous day. And I was nervous. It’s sometimes hard for me to prepare myself to be around other people with ALS, people who are further progressed than I am. I was afraid that what was meant to be a day of fun and accomplishment was instead going to be wildly depressing.

I am happy to report that I was wrong. Read More>

On Doctors

I recently went to two starkly different doctors offices. The first was my regular ALS clinic here in San Francisco, where I saw myriad specialists, who poked at me and tested things like my breathing and my patience. I got a mostly good report, along with prescriptions for a new wheelchair and braces to wear during the day that will keep my ankles from turning in and looking like they’re broken, which is sort of a horrifying way for them to look. They don’t hurt. Rob was told that he has to massage my feet twice a day, and I have no idea how we’re going to fit that into our busy morning of trying to encourage Scarlett to put clothes on her body and maybe even eat food before she goes off to summer camp. In fact, I’m 100% sure there will be no morning foot massages. So maybe we’ll just aim for once a day. Read More>